Quality risk management for cleanroom garment qualification in the light of GMP Annex 1

Helping you to understand key QRM principles for cleanroom garments

According to current GMP guidelines all aseptic manufacturing of sterile products should be managed by applying Quality Risk Management principles, that provide a proactive means of identifying, scientifically evaluating and controlling potential risks to quality. Because many factors contribute to the overall quality and suitability of cleanroom garment systems, the cleanroom garment qualification process is very important. During the webinar you will have the unique chance to learn about QRM principles for cleanroom garments, understand contamination risks as well as validation processes, all in the light of the latest draft of GMP Annex 1.